Cyclopenta[c]pyran-3(1H)-one, hexahydro-6-methylene-, (4aR,7aR)-rel- (9CI)

Base Information

Chemical Name:Cyclopenta[c]pyran-3(1H)-one, hexahydro-6-methylene-, (4aR,7aR)-rel- (9CI)
CAS No.:600700-71-8
Molecular Formula:C9H12O2
Molecular Weight:152.19
Hs Code.:
Mol file:600700-71-8.mol

Synonyms:Cyclopenta[c]pyran-3(1H)-one, hexahydro-6-methylene-, (4aR,7aR)-rel- (9CI)

Suppliers and Price of Cyclopenta[c]pyran-3(1H)-one, hexahydro-6-methylene-, (4aR,7aR)-rel- (9CI)

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Cyclopenta[c]pyran-3(1H)-one, hexahydro-6-methylene-, (4aR,7aR)-rel- (9CI)

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Technology Process of Cyclopenta[c]pyran-3(1H)-one, hexahydro-6-methylene-, (4aR,7aR)-rel- (9CI)

There total 2 articles about Cyclopenta[c]pyran-3(1H)-one, hexahydro-6-methylene-, (4aR,7aR)-rel- (9CI) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 74.0%

: 1779-49-3
Methyltriphenylphosphonium bromide

: 145448-46-0
cis-3-Oxabicyclo<4.3.0>-nonane-4,8-dione

: 600700-71-8
cis-hexahydro-5-methylenecyclopenta[c]pyran-3(1H)-one

Guidance literature:: Methyltriphenylphosphonium bromide; With potassium tert-butylate; In tetrahydrofuran; at 20 ℃; for 0.5h;

cis-3-Oxabicyclo<4.3.0>-nonane-4,8-dione; In tetrahydrofuran; at 20 ℃; for 3h;
DOI:10.1021/acs.joc.9b01589

Reference yield: 43.0%

: 100812-69-9
cis-hexahydro-5-methylene-2(1H)-pentalenone

: 600700-71-8
cis-hexahydro-5-methylenecyclopenta[c]pyran-3(1H)-one

Guidance literature:: With CHMO-expressing recombinant cells; β‐cyclodextrin; In various solvent(s); at 20 ℃; Microbiological reaction;
DOI:10.1002/ejoc.200300023